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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060746Generated: October 31, 2026

Allyl Alcohol → HCID 13005704, compound

https://huagongshe.com/reaction/2060746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium HydroxideHCID 14798—
ReactantTetrabutylammoniumHCID 16028—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 13005704HCID 13005704109.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

Tetrabutylammonium hydrogenosulfate (470 g, 1.40 mol) is added to a solution of sodium hydroxide (6.6 Kg, 165 mol) in water (14 L) and toluene (14 L) at 20° C. Allyl alcohol (801.5 g, 13.8 mol) is added and the mixture is stirred at 20° C. for 1 h. The mixture is cooled to 5° C., and tert-butyl 2-bromoacetate (4 Kg, 20.5 mol) is added slowly maintaining the internal temperature below 15° C. The reaction mixture is stirred at room temperature for 16 h. The mixture is diluted with water (12 L) and hexanes (12 L) and the organic phase is separated. The aqueous phase is extracted with MTBE (5 L). The combined organic phase is dried over magnesium sulfate, filtered, and concentrated to afford the title compound as colorless oil (2.6 Kg, 100%). ES/MS m/e: 173 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278441B2
Source datasetuspto-grants-2012_10
ORD IDord-3cc4a2cda5ea41469ea6788e45be7925
Source noteuspto-grants-2012_10